- ►hematologylibrary.org - Free from Publisher DA Weinstein, CN Roy, MD Fleming, MF Loda, … - Blood, 2002 - bloodjournal.hematologylibrary.org The erythroid bone marrow requires a large, continuous supply of iron to make
normal red blood cells. This iron comes from 2 sources. A small portion enters
the body each day through intestinal absorption of dietary iron. A much ... Cited by 337 - Related articles - BL Direct - All 7 versions
CS Grant - Baillière's clinical gastroenterology, 1996 - Elsevier Fundamental to establishing a diagnosis of insulinoma is first to consider the
diagnosis when presented with the constellation of symptoms and signs that
indicate hypoglycaemia. Prominent and most convincing are manifestations of ... Cited by 224 - Related articles - BL Direct - All 10 versions
- ►rsna.org L Grazioli, MP Federle, G Brancatelli, T … - Radiographics, 2001 - radiographics.rsna.org 1 From the Department of Radiology, University of Brescia, Brescia, Italy (LG);
the Department of Radiology, University of Pittsburgh Medical Center,
Presbyterian Hospital, 200 Lothrop St, Rm 4660 CHP MT, Pittsburgh, PA 15213 ... Cited by 116 - Related articles - BL Direct - All 4 versions
P Labrune, P Trioche, I Duvaltier, P Chevalier, … - Journal of pediatric gastroenterology and nutrition, 1997 - journals.lww.com Background: Hepatocellular adenomas may develop in patients with glycogen
storage disease types I and III, and the malignant degeneration of adenomas in
hepatocellular carcinoma has been reported in ten cases. The aim of this ... Cited by 94 - Related articles - BL Direct - All 3 versions
G Visser, JP Rake, J Fernandes, P Labrune, … - The Journal of pediatrics, 2000 - Elsevier From Beatrix Children's Hospital, University Hospital, Groningen, The
Netherlands; Hospital Antoine-Béclère, Clamart, France; the Institute of Child
Health, Great Ormond Street Hospital, London, United Kingdom; the ... Cited by 67 - Related articles - BL Direct - All 7 versions
- ►ufrgs.br [PDF] JP Rake, G Visser, P Labrune, JV Leonard, K … - European journal of pediatrics, 2002 - Springer Abstraet Glycogen storage disease type I (GSD I) is a relatively rare metabolic
disease and therefore, no meta- bolic centre has experience of large numbers of
patients. To document outcome, to develop guidelines about (long- term) ... Cited by 61 - Related articles - BL Direct - All 7 versions
JI Wolfsdorf, IA Holm, DA Weinstein - Endocrinology and metabolism clinics of North America, 1999 - Elsevier Glycogen synthesis and degradation in the liver follow distinct pathways that
begin and end with glucose-1-phosphate (Fig. 1). 70 The liver is freely
permeable to glucose, which is converted first to glucose-6-phosphate (G6P) ... Cited by 49 - Related articles - BL Direct - All 4 versions
L Faivre, D Houssin, J Valayer, J Brouard, M … - Journal of inherited metabolic disease, 1999 - Springer Page 1. J. Inher. Metab. Dis. 22 723»732 (1999) SSIEM and Kluwer Academic
Publishers. Printed in the Netherlands ( Long-term outcome ... Cited by 42 - Related articles - BL Direct - All 6 versions
- ►bloodjournal.org S Calderwood, L Kilpatrick, SD Douglas, M … - Blood, 2001 - Am Soc Hematology Glycogen storage disease (GSD) type 1b results from a deficiency of the
glucose-6-phosphate translocase enzyme. This enzyme transports
glucose-6-phosphate into the lumen of the endoplasmic reticulum, where it ... Cited by 40 - Related articles - BL Direct - All 6 versions
